Method of electroplating photoresist defined features from copper electroplating baths containing reaction products of alpha amino acids and bisepoxides

US2017037527A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2017037527-A1
Application numberUS-201615220472-A
CountryUS
Kind codeA1
Filing dateJul 27, 2016
Priority dateAug 6, 2015
Publication dateFeb 9, 2017
Grant date

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

Official abstract text for this publication.

Electroplating methods enable the plating of photoresist defined features which have substantially uniform morphology. The electroplating methods include copper electroplating baths with reaction products of α-amino acids and bisepoxides to electroplate the photoresist defined features. Such features include pillars, bond pads and line space features.

First claim

Opening claim text (preview).

What is claimed is: 1 . A method comprising: a) providing a substrate comprising a layer of photoresist, wherein the layer of photoresist comprises a plurality of apertures; b) providing a copper electroplating bath comprising one or more reaction products of one or more α-amino acids and one or more bisepoxides; an electrolyte; one or more accelerators; and one or more suppressors; c) immersing the substrate comprising the layer of photoresist with the plurality of apertures in the copper electroplating bath; and d) electroplating a plurality of copper photoresist defined features in the plurality of apertures, the plurality of photoresist defined features comprise an average % TIR of -5% to -1%. 2 . The method of claim 1 , wherein an average % WID of an array of copper photoresist defined features on the substrate is 12% to 15%. 3 . The method of claim 1 , wherein the one or more α-amino acids are chosen from arginine and lysine. 4 . The method of claim 1 , wherein the one or more bisepoxides have a formula: wherein R 1 and R 2 are independently chosen from hydrogen and (C 1 -C 4 )alkyl, A=O((CR 3 R 4 ) m O) n or (CH 2 ) y , each R 3 and R 4 is independently chosen from hydrogen, methyl, or hydroxyl, m=1-6, n=1-20 and y=0-6 and when y=0, A is a chemical bond. 5 . The method of claim 4 , wherein the bisepoxides have a formula: wherein R 1 and R 2 are independently chosen from hydrogen and (C 1 -C 4 )alkyl, R 3 and R 4 are chosen from hydrogen, methyl or hydroxyl, m=1-6, n=1. 6 . The method of claim 1 , wherein the one or more reaction products are in amounts of 0.25 ppm to 20 ppm in the copper electroplating bath. 7 . The method of claim 1 , wherein electroplating is done at a current density of 0.25 ASD to 40 ASD. 8 . The method of claim 1 , wherein the one or more copper photoresist defined features are pillars, bond pads or line space features. 9 . A plurality of photoresist defined features on a substrate comprising an average % TIR of −5% to −1% and an average % WID of 12% to 15%.

Assignees

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Classifications

  • of bump connectors, dummy bumps or thermal bumps · CPC title

  • by using masks · CPC title

  • by plating, e.g. electroless plating or electroplating · CPC title

  • by using masks · CPC title

  • Plan-view shape, i.e. in top view · CPC title

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What does patent US2017037527A1 cover?
Electroplating methods enable the plating of photoresist defined features which have substantially uniform morphology. The electroplating methods include copper electroplating baths with reaction products of α-amino acids and bisepoxides to electroplate the photoresist defined features. Such features include pillars, bond pads and line space features.
Who is the assignee on this patent?
Rohm & Haas Elect Mat, Dow Global Technologies Llc
What technology area does this patent fall under?
Primary CPC classification C25D3/38. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Feb 09 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).